A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010667



Internal ID74739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38340200..38340233hg38UCSC Ensembl
chr8:38197718..38197751hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544214
Supporting Variants
Samples
Known GenesWHSC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010667
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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